Genetics

Genomic consent: New guideline to help researchers and patients

How can Canada optimize the impact of human genomic sequencing to increase our understanding of disease? New guidance in Canadian Medical Association Journal (CMAJ) lays out the key elements for obtaining patient consent ...

Diseases, Conditions, Syndromes

CRISPR treatment slows swelling in hereditary angioedema patients

Hereditary angioedema (HAE) is a rare, genetic disorder characterized by severe, recurring, and unpredictable swelling attacks in various organs and tissues of the body, which can be painful, debilitating, and life-threatening. ...

Genetics

Mutation in TLR7 increases risk of severe COVID-19

Rare gene mutations can significantly increase the risk of severe COVID-19 disease. An international research team with significant contribution from the University of Bonn compared the genetic material of 5,085 people with ...

Genetics

Sharing variant information to improve diagnosis

A national platform for diagnostic laboratories to share genetic evidence and build consistent interpretations of that information is paving the way for more accurate diagnosis of patient conditions.

Diseases, Conditions, Syndromes

Researchers reveal why shingles can lead to stroke

Scientists investigating why people who have had shingles are at a higher risk of stroke, now believe the answer lies within lipid vesicles called exosomes that shuttle proteins and genetic information between cells, according ...

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